ClinGen Allele Registry
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Canonical Allele Identifier:
PA915964541
Gene: APOB
HGNC
NCBI
Linked Data
ClinVar Variation Id:
237738
ClinVar RCV Id:
RCV000606261
RCV000584100
RCV000758755
RCV000771081
RCV001139000
RCV001138999
RCV001837770
RCV002372257
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000375.3:p.Val4265Ala
CA051139
NM_000384.3:c.12794T>C